| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:94459652-94460079 | Common:6; Rare:122 | ||||
| chr12:94615982-94616166 | Rare:35 | ||||
| chr12:95003594-95003835 | Common:3; Rare:101; Clinvar (benign):6 | ||||
| chr12:95073413-95073658 | Common:2; Rare:83 | ||||
| chr12:95217367-95217890 | Common:5; Rare:139 | ||||
| chr12:95218143-95218316 | Common:2; Rare:44 | ||||
| chr12:95295858-95296095 | Common:1; Rare:43 | ||||
| chr12:95474037-95474330 | Common:2; Rare:123 | ||||
| chr12:95548788-95548958 | Common:3; Rare:51 | ||||
| chr12:95790249-95790409 | Common:2; Rare:50 | ||||
| chr12:95858822-95859076 | Common:3; Rare:74 | ||||
| chr12:95996288-95996506 | Common:2; Rare:39; Clinvar:1; Clinvar (benign):1 | ||||
| chr12:96035360-96035452 | Common:1; Rare:25 | ||||
| chr12:96255330-96255485 | Common:1; Rare:34 | ||||
| chr12:96399371-96399463 | Common:1; Rare:25 |